T108R (p.Thr108Arg) variant of HSD17B3 (P37058)
T108R (p.Thr108Arg) in HSD17B3 (P37058) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
T108R (p.Thr108Arg) variant details
- p.Thr108Arg
- NCI-TCGA Cosmic COSV1009
- cosmic curated COSV10093
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.84
- MetaSVM 0.83
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available